Autism and Sen in Fiction: Guest Post – What Jennifer Knows by Wendy James

Reposted from Jera’s Jamboree.co.uk.

Shaz Goodwin says:  

When Wendy contacted me to guest on JJ about Autism and Special Educational Needs and Disability (SEND) in fiction I knew that we would be a good ‘fit’ for each other.  I have a great deal of admiration for what she does for families and am honoured to be able to share her guest post with you today.

Wendy lives in London with her husband and youngest son. A number of her short stories have recently appeared in anthologies, and 2015 sees the launch of her first solo novel, What Jennifer Knows. Her writing is inspired by family, friends, and everyday events that only need a little twist to become entertaining fiction.

As well as writing contemporary fiction, she loves to read it too, and spreads the word about good books online and in the real world.

Wendy is also a freelance proofreader, and a caseworker for The National Autistic Society’s Education Rights Service.

You can connect with Wendy on social media via Twitter @wendyproof, her Facebook author pageGoogle+ and Goodreads Author page.

by Wendy Janes

One of the subplots in my book, What Jennifer Knows, involves Jennifer’s young grandson, Tim. He’s having problems at school and she suspects he’s on the autism spectrum.

Autism and special educational needs are subjects that are personally and professionally important to me. My youngest son (20) is on the spectrum and I’m a caseworker for The National Autistic Society’s Education Rights Service.

We are a small part of The National Autistic Society’s vast selection of services in the UK. Via phone and email we offer advice to parents of children with a diagnosis (or about to receive a diagnosis) of autism on how to ensure that their children receive appropriate support to achieve their full educational potential.

Although many schools do provide children with an excellent education that meets their needs, some schools lack the skills, willingness or resources, and as a result, children and their families suffer. The impact of unmet needs can be huge: hours, days, weeks and months of lost education, days and nights of anxiety and upset.

I’ve been incredibly moved by some of the things I’ve heard, but in order to help families, we empathise with their distress and concentrate on giving them the tools to negotiate through to a solution. Turning a situation of conflict into cooperation can take time and patience, but I always believe it’s achievable. We use the law, regulations and guidance to empower parents, but don’t suggest they wade in and accuse schools of failing in their legal duties. The focus must be on the child, with schools and parents trusting, respecting and listening to each other.

In the early chapters of my story, Tim’s mother, Blythe appears uncooperative, critical, fighting the people who could help her, but really she’s scared. It feels to her as though the school staff are criticising her parenting, but worse than that, she believes they don’t even like her child. Her response is to attack them back.

I speak to many parents who feel like Blythe does, and if I can help them in even a tiny way by allowing them a safe space to express their worries, or by indicating a way forward, or giving them the confidence to negotiate and advocate for their child, I’ll have done my job. It’s a privilege to be able to help.

I also believe it’s a privilege and a responsibility to write about special educational needs and autism in my fiction. And for me, that involves ensuring that the inclusion feels respectful, natural, not tacked-on to the story for the sake of drama, and it begins with getting the facts right.

To quote from The National Autistic Society’s website:

“Autism is a lifelong developmental disability that affects how a person communicates with, and relates to, other people. It also affects how they make sense of the world around them.”
As it’s a spectrum, it means that people with the diagnosis share certain similar difficulties, but they are affected in different ways. I’m constantly amazed at how my introverted and quietly spoken son has the same diagnosis as one of his friends who is a whirlwind of loud chatter. And they share the same umbrella as someone who has no functional speech at all. I’ve been particularly fascinated by the fact that someone on the spectrum who uses language fluently won’t necessarily understand all its nuances, and that someone who has no functional speech could have plenty to say.

I’ll never forget a video I watched a few years ago where a young man, who could only make what sounded to me like strange noises, was given a laptop, and I cried as he typed the words he couldn’t voice. I cried for the beauty and fluency of his language and for all the negative presumptions I’d made about him.

It would be unrealistic to make Tim in my story represent all the children on the vast spectrum. Tim’s an individual who isn’t solely defined by his pending diagnosis. He’s a little boy with strengths and weaknesses, who, at the start of the book, is going through a tough time that’s affecting his whole family.

I’d like to think that the small strand in my story about Tim is giving a voice to children with autism and their families, gently asking for understanding and a little compassion.

If you’d like to read more about autism, here’s a link to The National Autistic Society’s What is autism? page on their website: http://www.autism.org.uk/about-autism/introduction/what-is-autism.aspx

Thank you for sharing Wendy.  And for the reminder of how we might make judgements from our own perceptions that may not necessarily be true.

A ‘spectrum’ is defined as being “used to classify something in terms of its position on a scale between two extreme points.”  I think the changes to diagnostic criteria reflect this scale and in my opinion, the most beneficial change is (as quoted from The National Autistic Society):
The emphasis during diagnosis will change from giving a name to the condition to identifying all the needs someone has and how these affect their life.
It changes perceptions and judgements away from ‘labelling’ towards the actual needs of the child/young person/adult and what can we do to meet those needs.  From my point of view, it’s not first and foremost about applying for an assessment for an Education and Health Care Plan (although that may be an outcome) but how we can make the school day less anxious and isolating and more inclusive.  A label is limiting whereas we should be looking at children holistically so that they can be who they are in the situations they find themselves.  Rant over 🙂

Below is Wendy’s novel, What Jennifer Knows.

What Jennifer Knows

Trailer

A vital member of her Surrey community, Jennifer Jacobs is dedicated to her job as a dance therapist, helping children with special needs to express themselves through movement. Wife of a successful though reclusive sculptor, Gerald, she is known for having a deep sense of empathy, making her a trusted confidante. So when two very different friends, Freya and Abi, both share information with her that at first seems to be an awkward coincidence, she doesn’t tell them. But as the weeks roll by, the link revealed between the two women begins to escalate into a full-blown moral dilemma – and also brings to the surface a painful memory Jennifer believed she had long since forgotten. What is the right thing to do? Should she speak out or is the truth better left unsaid?

Amazon author page UK

Amazon author page US

Posted by Shaz Goodwin at Thursday, November 26, 2015

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Labels: AUTISMGUEST POSTINDIE AUTHORSEN-DWENDY JANESWHAT JENNIFER KNOWS

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